HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798670Generated: November 1, 2026
2-Methyl-3-butyn-2-ol → 4-Hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one
https://huagongshe.com/reaction/1798670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | N,4-Dimethoxy-N-methylbenzamide | HCID 15105748 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one | HCID 12722577 | 81% |
Reaction Steps
To a stirred solution of 2-methylbut-3-yn-2-ol (2.15 g, 25.6 mmol) in dry THF (80 mL) was added n-BuLi (24.0 mL, 38.7 mmol, 1.6 M in hexane) drop wise at −20° C. under an inert atmosphere for a period of 10 min. After being stirred for 30 min at −20° C., a solution of N,4-dimethoxy-N-methylbenzamide (2.5 g, 12.8 mmol) in dry THF (10 mL) was added to reaction mixture and stirring was continued for an additional 3 h at −20° C. The reaction mixture was quenched with a saturated NH4Cl solution and extracted with EtOAc (2×100 mL). The combined organic layer was washed with water (100 mL), brine (40 mL), dried over Na2SO4, filtered and concentrated in vacuo to afford 4-hydroxy-1-(4-methoxyphenyl)-4-methylpent-2-yn-1-one (2.25 g, 81%) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343973B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c387af050c57463bb4781fbf52993b46 |
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| Source note | uspto-grants-2013_01 |
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